Evidence map›Paper›PMID 35999479›Full record

ArticleMolecular biotechnology2023

DEAE-Dextran Enhances the Lentiviral Transduction of Primary Human Mesenchymal Stromal Cells from All Major Tissue Sources Without Affecting Their Proliferation and Phenotype.

Francesco Amadeo, Vivien Hanson, Patricia Murray, Arthur Taylor

Open access · hybridAbstract read
In one paragraph

Article in Molecular biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. An optimizing lentiviral titer determination assay based on Raji cells.American journal of translational research · 2025
    Article
  3. Identification of a small molecule for enhancing lentiviral transduction of T cells.Molecular therapy. Methods & clinical development · 2023
    Article
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Francesco AmadeoCellular Therapies Laboratory, NHS Blood and Transplant, Liverpool, UK.ORCID http://orcid.org/0000-0002-3868-2348
Vivien HansonCellular Therapies Laboratory, NHS Blood and Transplant, Liverpool, UK.
Patricia MurrayDepartment of Molecular Physiology and Cell Signalling, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0003-1316-148X
Arthur TaylorDepartment of Molecular Physiology and Cell Signalling, University of Liverpool, Liverpool, UK. taylora@liverpool.ac.uk.ORCID http://orcid.org/0000-0003-2028-6694
NHS Blood and Transplant · GBUniversity of Liverpool · GB

Funding

H2020 Marie Skłodowska-Curie Actions 813839
6 · The paper itself

Abstract

Genetic engineering of mesenchymal stromal cells (MSCs) is a tool widely used to explore MSC properties in vitro and in vivo. Lentiviral infection with the use of polycations as an adjuvant is a method that is commonly used to generate stably transduced cells. However, it is known that some polycations can negatively affect primary MSCs and to date, no study has explored the effect of different polycations on the transduction efficiency and properties of all main types of MSCs, namely those derived from umbilical cord, bone marrow and adipose tissue. Here we explore a range of polycations, using transduction protocols with and without spinoculation, to produce stably transduced MSCs from these three tissue sources. We identified that an overnight incubation with diethylaminoethyl-dextran (DEAE-Dextran) is the protocol associated with the best transduction efficiency without compromising the viability of the cells, and which worked consistently with lentiviral particles encoding for different transgenes. Transduced and sorted MSC populations revealed no significant changes in proliferation, morphology and expression of MSC markers compared to naïve MSCs. Following this study, we conclude that DEAE-Dextran is a polycation that can be successfully used to enhance the transduction of MSCs from all major tissue sources.

Indexed as

DEAE-DextranMesenchymal Stem CellsCell DifferentiationCell ProliferationCells, CulturedGenetic VectorsHumansLentivirusPhenotypePolyelectrolytesTransduction, GeneticDEAE-DextranPolyelectrolytesLentivirusMesenchymal stromal cellsPolycationsReporter genesTransduction

Identifiers

PMID35999479
PMCPMC9974715
OpenAlexW4292847471

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.